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The bobtail or brachyury trait is caused by an autosomal dominant mutation in the T-box transcription factor T (TBXT) gene.
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Caractéristiques
| Breeds | Berger américain miniature, Berger australien, Berger des Pyrénées, Bouvier australien courte queue, Braque du Bourbonnais, Brittany, Chien d’eau espagnol, Chien de ferme dano-suédois, Croatian Sheepdog, Mudi, Polish Lowland Sheepdog, Swedish Vallhund, Terrier brésilien, Jack Russell Terrier, Schipperke, Welsh Corgi Pembroke |
|---|---|
| Gene | |
| Organ | |
| specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
| Mode of Inheritance | |
| Chromosome | |
| Also known as | |
| Year Published |
Informations générales
The bobtail or brachyury trait is caused by an autosomal dominant mutation in the T-box transcription factor T (TBXT) gene. The TBXT or T-gene encodes transcription factors that play critical roles in embryonic development, especially the tail and spine. A single copy of the mutation (heterozygous) causes the bobtail look, but two copies (homozygous mutant) disrupt development so severely that the embryo cannot survive. This makes the mutation homozygous lethal.
The tested mutation was originally discovered in the Pembroke Welsh Corgi, but also causes distinctive short tails in multiple other breeds, mainly sheepdogs and hunting breeds.
Caractéristiques cliniques
Dogs with one copy of the mutation have a naturally short or missing tail. If a puppy inherits two copies (homozygous mutant), it usually dies before birth due to the complete turn-off of the gene.
Additional Information
The T gene mutation is not present in all breeds of short-tailed dogs, and therefore another genetic factor is possible affecting the tail phenotype in for example Spaniels, Schnauzers and Rottweilers.
Références
Pubmed ID: 11252170
Omia ID: 975